List of works - Camila Lopes Veronez

A new mutation in the SERPING1 gene in a Brazilian family with hereditary angioedema.

scientific article published on 8 April 2015

A rare mutation in the F12 gene in a patient with ACE inhibitor-induced angioedema.

scientific article published on 5 May 2017

Abstracts from the 10th C1-inhibitor deficiency workshop.

scientific article

Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis.

scientific article

Endothelial B2-receptor overexpression as an alternative animal model for hereditary angioedema

scientific article published on 28 June 2019

Genetic Variation of Kallikrein-Kinin System and Related Genes in Patients With Hereditary Angioedema

article

Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencing

scientific article published in April 2016

Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families

scientific article published on 8 November 2017

Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio-oedema.

scientific article published on 22 September 2015

International Consensus on the Use of Genetics in the Management of Hereditary Angioedema

scientific article published on 24 October 2019

Mycoplasma hyopneumoniae in vitro peptidase activities: identification and cleavage of kallikrein-kinin system-like substrates.

scientific article

New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema

article

P-I class metalloproteinase from Bothrops moojeni venom is a post-proline cleaving peptidase with kininogenase activity: insights into substrate selectivity and kinetic behavior.

scientific article

Reply

SERPING1 mutation in a rare hereditary angioedema with skin blisters.

scientific article published on 30 November 2018

Targeted Next-Generation Sequencing in Brazilian Children With Nephrotic Syndrome Submitted to Renal Transplant

scientific article published on 28 June 2017

The involvement of proteoglycans in the human plasma prekallikrein interaction with the cell surface.

scientific article

Use of pdC1-INH concentrate for long-term prophylaxis during pregnancy in hereditary angioedema with normal C1-INH.

scientific article published on 10 February 2018

List of works by Camila Lopes Veronez

A new mutation in the SERPING1 gene in a Brazilian family with hereditary angioedema.

A rare mutation in the F12 gene in a patient with ACE inhibitor-induced angioedema.

Abstracts from the 10th C1-inhibitor deficiency workshop.

Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis.

Endothelial B2-receptor overexpression as an alternative animal model for hereditary angioedema

Genetic Variation of Kallikrein-Kinin System and Related Genes in Patients With Hereditary Angioedema

Genetic analysis of hereditary angioedema in a Brazilian family by targeted next generation sequencing

Hereditary Angioedema with Normal C1 Inhibitor and F12 Mutations in 42 Brazilian Families

Homozygosity for a factor XII mutation in one female and one male patient with hereditary angio-oedema.

International Consensus on the Use of Genetics in the Management of Hereditary Angioedema

Mycoplasma hyopneumoniae in vitro peptidase activities: identification and cleavage of kallikrein-kinin system-like substrates.

New mutations in SERPING1 gene of Brazilian patients with hereditary angioedema

P-I class metalloproteinase from Bothrops moojeni venom is a post-proline cleaving peptidase with kininogenase activity: insights into substrate selectivity and kinetic behavior.

Reply

SERPING1 mutation in a rare hereditary angioedema with skin blisters.

Targeted Next-Generation Sequencing in Brazilian Children With Nephrotic Syndrome Submitted to Renal Transplant

The involvement of proteoglycans in the human plasma prekallikrein interaction with the cell surface.

Use of pdC1-INH concentrate for long-term prophylaxis during pregnancy in hereditary angioedema with normal C1-INH.